Gitelman syndrome combined with growth hormone deficiency: Three cases report

RATIONALE: Gitelman syndrome (GS) is a rare autosomal recessive hereditary salt-losing tubulopathy caused by loss-of-function mutations in the SLC12A3 gene. It is usually characterized by hypokalemia, metabolic alkalosis, hypomagnesemia, and hypocalciuria. There are only a few reports on GS combined...

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Publicat a:Medicine (Baltimore)
Autors principals: Huang, Ke, Dai, Yang-Li, Zhang, Jian-Wei, Zhang, Li, Wu, Wei, Dong, Guan-Ping, Ullah, Rahim, Fei, Yue, Fu, Jun-Fen
Format: Artigo
Idioma:Inglês
Publicat: Wolters Kluwer Health 2019
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4300
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6783222/
https://ncbi.nlm.nih.gov/pubmed/31577716
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000017244
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